6JUT: ZAK

Crystal structure of ZAK in complex with compound 6k. Determined by X-ray diffraction at 2.1 Å resolution. Released 24 Jul 2019.

Method: X-ray diffraction
Resolution: 2.1 Å
Organism: Homo sapiens
Chains: 1
Atoms: 2,515
Mol. weight: 35.9 kDa
Ligands: C9O
Released: 24 Jul 2019

Explore 6JUT in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

6JUT contains 21 α-helices and 10 β-strands across 1 chain. Residue ranges use author residue numbering, as in the PDB file, from PDBe. To see them in 3D, choose the Cartoon representation with Secondary structure coloring: helices, sheets and coils get different colors.

Chain A: 21 helices, 10 β-strands

Element	Residues	Length	Sheet
β-strand	10-11	2	1
α-helix	13-15	3
β-strand	16-21	6	1
β-strand	30-35	6	1
β-strand	40-47	8	1
α-helix	52-57	6
β-strand	65	1	2
α-helix	66-67	2
β-strand	68-74	7	1
β-strand	77-83	7	1
β-strand	89	1	2
α-helix	90-94	5
α-helix	97-101	5
α-helix	104-119	16
α-helix	120-124	5
α-helix	136-138	3
β-strand	139-141	3	2
β-strand	147-149	3	2
α-helix	154-157	4
α-helix	163-166	4
α-helix	170-172	3
α-helix	175-178	4
α-helix	187-201	15
α-helix	211-219	9
α-helix	225-228	4
α-helix	233-242	10
α-helix	247-249	3
α-helix	251-252	2
α-helix	253-263	11
α-helix	269-277	9
α-helix	280-303	24

Molecules and chains

Molecule	Chains	Type	Length	Organism	UniProt
Mitogen-activated protein kinase kinase kinase MLT	A	protein	310	Homo sapiens	Q9NYL2 (AlphaFold model)

Sequence of entity 1 (A), FASTA

>6JUT_1 Mitogen-activated protein kinase kinase kinase MLT (chains A)
GAMGSGASFVQIKFDDLQFFENCGGGSFGSVYRAKWISQDKEVAVKKLLKIEKEAEILSV
LSHRNIIQFYGVILEPPNYGIVTEYASLGSLYDYINSNRSEEMDMDHIMTWATDVAKGMH
YLHMEAPVKVIHRDLKSRNVVIAADGVLKICDFGASRFHNHTTHMSLVGTFPWMAPEVIQ
SLPVSETCDTYSYGVVLWEMLTREVPFKGLEGLQVAWLVVEKNERLTIPSSCPRSFAELL
HQCWEADAKKRPSFKQIISILESMSNDTSLPDKCNSFLHNKAEWRCEIEATLERLKKLER
DLSFKEQELK

Ligands and cofactors

ID	Name	Formula	Copies
C9O	~{N}-[2,4-bis(fluoranyl)-3-[4-(3-methoxy-1~{H}-pyrazolo[3,4-b]pyridin-5-yl)-1,2…	C21 H14 Br F2 N7 O3 S	1

Primary citation

Design, Synthesis, and Structure-Activity Relationships of 1,2,3-Triazole Benzenesulfonamides as New Selective Leucine-Zipper and Sterile-alpha Motif Kinase (ZAK) Inhibitors. Yang, J., Shibu, M.A., Kong, L. et al. J Med Chem (2020) 63:2114-2130. DOI 10.1021/acs.jmedchem.9b00664 · PubMed

Other PDB entries of the same protein (UniProt Q9NYL2 (AlphaFold model), which also has an AlphaFold model), best resolution first:

5X5O 1.87 Å, Crystal structure of ZAK in complex with compound D2829
6JUU 1.9 Å, Crystal structure of ZAK in complex with compound 6r
7YAW 2.1 Å, Crystal structure of ZAK in complex with compound YH-180
5HES 2.14 Å, Human leucine zipper- and sterile alpha motif-containing kinase (ZAK, MLT, HCCS-4, MRK,…
9RPV 2.35 Å, Structure of the ZAK-bound human disome
7YAZ 2.54 Å, Crystal structure of ZAK in complex with compound YH-186
9RSX 2.91 Å, Structure of RACK1 bound to the C-terminus of SERBP1 and the RIH region of ZAK

Browse structure collections

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